RCOR2[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2455394	NM_173587.4(RCOR2):c.1517A>C (p.Gln506Pro)	RCOR2 (Q506P)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2279634	NM_173587.4(RCOR2):c.1504C>G (p.Arg502Gly)	RCOR2 (P425R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300401	NM_173587.4(RCOR2):c.1502C>T (p.Ala501Val)	RCOR2 (A501V)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2522621	NM_173587.4(RCOR2):c.1460C>T (p.Pro487Leu)	RCOR2 (P487L)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2393904	NM_173587.4(RCOR2):c.1385C>A (p.Thr462Asn)	RCOR2 (T462N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513100	NM_173587.4(RCOR2):c.1352C>T (p.Pro451Leu)	RCOR2 (P451L)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2515845	NM_173587.4(RCOR2):c.1292G>A (p.Arg431Gln)	RCOR2 (R431Q)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2337000	NM_173587.4(RCOR2):c.1291C>G (p.Arg431Gly)	RCOR2 (R431G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618580	NM_173587.4(RCOR2):c.1232C>T (p.Ala411Val)	RCOR2 (A411V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305049	NM_173587.4(RCOR2):c.1153G>A (p.Glu385Lys)	RCOR2 (E385K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619750	NM_173587.4(RCOR2):c.899G>A (p.Ser300Asn)	RCOR2 (S300N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313437	NM_173587.4(RCOR2):c.812C>A (p.Thr271Lys)	RCOR2 (T271K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313436	NM_173587.4(RCOR2):c.811A>G (p.Thr271Ala)	RCOR2 (T271A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313435	NM_173587.4(RCOR2):c.766C>T (p.Arg256Trp)	RCOR2 (R256W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540299	NM_173587.4(RCOR2):c.742T>C (p.Tyr248His)	RCOR2 (Y248H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537431	NM_173587.4(RCOR2):c.703C>T (p.Arg235Cys)	RCOR2 (R235C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409613	NM_173587.4(RCOR2):c.652G>C (p.Asp218His)	RCOR2 (D218H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396420	NM_173587.4(RCOR2):c.626G>A (p.Arg209Gln)	RCOR2 (R209Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508364	NM_173587.4(RCOR2):c.625C>G (p.Arg209Gly)	RCOR2 (R209G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246028	NM_173587.4(RCOR2):c.541A>G (p.Ser181Gly)	RCOR2 (S181G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517426	NM_173587.4(RCOR2):c.513A>C (p.Lys171Asn)	RCOR2 (K171N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458770	NM_173587.4(RCOR2):c.437C>G (p.Ala146Gly)	RCOR2 (A146G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790098	NM_173587.4(RCOR2):c.319-8C>T	RCOR2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2399359	NM_173587.4(RCOR2):c.242A>G (p.Asn81Ser)	RCOR2 (N81S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152746	NM_173587.4(RCOR2):c.191C>T (p.Pro64Leu)	RCOR2 (P64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327101	NM_173587.4(RCOR2):c.130A>C (p.Ser44Arg)	RCOR2 (S44R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275443	NM_173587.4(RCOR2):c.88C>T (p.His30Tyr)	RCOR2 (H30Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534522	NM_173587.4(RCOR2):c.68T>C (p.Val23Ala)	RCOR2 (V23A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2252011	NM_173587.4(RCOR2):c.40A>T (p.Ile14Phe)	RCOR2 (I14F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152748	NM_173587.4(RCOR2):c.38G>C (p.Gly13Ala)	RCOR2 (G13A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152747	NM_173587.4(RCOR2):c.22C>G (p.Pro8Ala)	RCOR2 (P8A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31